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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 460351Erstellt: 24. Oktober 2026

Butanoic acid, 4-chloro-4-oxo-, methyl ester → 4-[3-(3-Fluoro-phenylamino)-6,7-dimethoxy-4H-indeno[1,2-c]pyrazol-1-yl]-4-oxo-butyric acid methyl ester

https://huagongshe.com/de/reaction/460351

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktButanoic acid, 4-chloro-4-oxo-, methyl esterHCID 73888—
EduktDiisopropylethylamineHCID 81531—
EduktJnj-10198409HCID 9797370—
LösungsmittelDimethylformamideHCID 6228—
Produkt4-[3-(3-Fluoro-phenylamino)-6,7-dimethoxy-4H-indeno[1,2-c]pyrazol-1-yl]-4-oxo-butyric acid methyl esterHCID 58824826—

Reaktionsschritte

To a mixture of (6,7-Dimethoxy-1,4-dihydro-indeno[1,2-c]pyrazol-3-yl)-(3-fluoro-phenyl)-amine (Compound 14) (0.50 g, 1.5 mmol), 3-Chlorocarbonyl-propionic acid methyl ester (Compound 26a) (0.277 g, 1.8 mmole) and DMF (1.5 mL) was added Diisopropylethylamine (DIEA) (0.52 mL, 3.0 mmole) at room temperature with stirring. The reaction was stirred at room temperature over night. The reaction was quenched with water and extracted with EtOAc. The solvent was removed via rotovap and the crude material was prepped on the reverse phase HPLC. Lyophilization gave the title compound as a white powder. MS m/z439.9 (M+H)+;

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07196110B2
Quelldatensatzuspto-grants-2007_03
ORD IDord-3032bbf713c84279888a4b6191ba6e7f
Quellennotizuspto-grants-2007_03